Shaun Purcell

Genetics · 2002–2018

A researcher in the Science corpus: 43 papers; trusts 9 researchers and is trusted by 23 researchers here, as inferred from the citation graph.

Subfields

Genetics — 625 citations into it; #679 of 6,854 by trust here, #10 by citations
Molecular Biology — 402 citations into it; #14,733 of 17,773 by trust here, #210 by citations

Whom Shaun Purcell trusts overall

Their strongest outbound trust, strongest first, inferred from their citations.

Who trusts Shaun Purcell overall

Papers from Shaun Purcell's perspective

Ordered by how strongly the researchers Shaun Purcell trusts endorse each paper. Same corpus, a different order for every researcher.

Genotype Imputation with Thousands of Genomes (G3: Genes, Genomes, Genetics)
Common SNPs explain a large proportion of heritability for human height (Nature Genetics)
Rare chromosomal deletions and duplications increase risk of schizophrenia (Nature)
10 Years of GWAS Discovery: Biology, Function, and Translation. (American Journal of Human Genetics)
FINEMAP: efficient variable selection using summary data from genome-wide association studies (bioRxiv)
Functional Impact of Global Rare Copy Number Variation in Autism Spectrum Disorder (Nature)
MAGMA: Generalized Gene-Set Analysis of GWAS Data (PLoS Comput. Biol.)
FTO Obesity Variant Circuitry and Adipocyte Browning in Humans (New England Journal of Medicine)
The support of human genetic evidence for approved drug indications (Nature Genetics)
Inherited determinants of Crohn's disease and ulcerative colitis phenotypes: a genetic association study (The Lancet)

Their papers

A second generation human haplotype map of over 3.1 million SNPs (2007) — 4,677 citations
PLINK: a tool set for whole-genome association and population-based linkage analyses. (2007) — 32,716 citations
Partitioning heritability by functional annotation using genome-wide association summary statistics (2015) — 2,445 citations
A framework for the interpretation of de novo mutation in human disease (2014) — 1,035 citations
Testing for an Unusual Distribution of Rare Variants (2011) — 617 citations
Gene Expression Elucidates Functional Impact of Polygenic Risk for Schizophrenia (2016) — 1,080 citations
Genome-wide association of early-onset myocardial infarction with common single nucleotide polymorphisms, common copy number variants, and rare copy number variants (2009) — 1,094 citations
De novo mutations in schizophrenia implicate synaptic networks (2014) — 1,622 citations
A polygenic burden of rare disruptive mutations in schizophrenia (2014) — 1,469 citations
Rare chromosomal deletions and duplications increase risk of schizophrenia (2008) — 1,525 citations
Genome-Wide Association Analysis Identifies Loci for Type 2 Diabetes and Triglyceride Levels (2007) — 2,928 citations
A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects: CNV Analysis Group and the Schizophrenia Working Group of the Psychiatric Genomics Consortium (2016) — 1,284 citations
The genetic architecture of type 2 diabetes (2016) — 1,066 citations
Pleiotropy in complex traits: challenges and strategies (2013) — 1,050 citations
Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores (2015) — 1,263 citations
Common variation in three genes, including a noncoding variant in CFH, strongly influences risk of age-related macular degeneration (2006) — 636 citations
Extremely low-coverage sequencing and imputation increases power for genome-wide association studies (2012) — 257 citations
Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depth. (2012) — 577 citations
Quantifying penetrance in a dominant disease gene using large population control cohorts (2016) — 400 citations
Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes (2018) — 667 citations